Response to Lenvatinib in Children with Papillary Thyroid Carcinoma

被引:20
|
作者
Mahajan, Priya [1 ]
Dawrant, Jonathan [5 ]
Kheradpour, Albert [6 ]
Quintanilla, Norma M. [2 ]
Lopez, Monica E. [3 ]
Orth, Robert C. [7 ]
Athanassaki, Ioanna [4 ]
Venkatramani, Rajkumar [1 ]
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, Div Hematol Oncol,Texas Childrens Canc Ctr, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Div Pediat Surg, Michael E DeBakey Dept Surg, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, Div Endocrinol, Houston, TX 77030 USA
[5] Alberta Childrens Prov Gen Hosp, Div Endocrinol, Dept Pediat, Calgary, AB, Canada
[6] Loma Linda Univ, Dept Pediat, Div Hematol Oncol, San Bernardino, CA USA
[7] Texas Childrens Hosp, Dept Radiol, Houston, TX 77030 USA
关键词
papillary thyroid carcinoma; lenvatinib; children; refractory; radioiodine-refractory thyroid carcinoma; cancer; FUSION ONCOGENES; YOUNG-ADULTS; CANCER; ADOLESCENTS; SORAFENIB; CHILDHOOD; MUTATIONS;
D O I
10.1089/thy.2018.0064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Papillary thyroid carcinoma (PTC) is the most common thyroid malignancy in children and adolescents. Infrequently, children with PTC may present with or develop disease not amenable to surgery or radioactive iodine (RAI), and systemic therapy may be an option. Lenvatinib is an oral tyrosine kinase inhibitor that is approved by the Food and Drug Administration for the treatment of adults with locally recurrent or metastatic, progressive, RAI-refractory well-differentiated thyroid carcinoma. The effect of lenvatinib in children with PTC has not been reported. Patient findings: Three children with metastatic PTC not amenable or refractory to RAI who responded to lenvatinib are reported. All of them developed respiratory distress requiring oxygen caused by extensive bilateral metastatic pulmonary disease. The first patient is a 14-year-old female who was initially treated with sorafenib for extensive PTC not amenable to upfront surgery or RAI. She had progressive pulmonary disease after five months, and was subsequently treated with oral lenvatinib (14 mg/m(2)/day). She was weaned to room air after eight weeks. The second patient is a 15-year-old male who was treated with lenvatinib (14 mg/m(2)/day) for iodine non-avid diffuse pulmonary disease after initial total thyroidectomy and cervical lymph node dissection. He was weaned off oxygen in six weeks. The third patient is a five-year-old male who was treated with lenvatinib (14 mg/m(2)/day) for pulmonary disease progression 24 months after treatment with total thyroidectomy, cervical lymph node dissection, and RAI treatment. He was weaned off oxygen one day after starting lenvatinib. Two of the patients required dose adjustments secondary to proteinuria. Otherwise, all patients tolerated lenvatinib well. The first two patients remained clinically stable on lenvatinib 23 months and 11 months after initiation of therapy, respectively, and the third patient transitioned to a tumor-specific targeted therapy after one month. Summary: Three pediatric patients are reported with metastatic PTC not amenable or refractory to RAI who achieved a response on lenvatinib. Conclusion: Lenvatinib therapy is well tolerated and demonstrated clinical activity in children with advanced PTC. Lenvatinib should be considered in children with PTC that is refractory or not amenable to conventional management.
引用
收藏
页码:1450 / 1454
页数:5
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